El-Sokkary G H
Department of Zoology, Faculty of Science, Assiut University, Assiut, Egypt.
Cell Prolif. 2008 Feb;41(1):168-76. doi: 10.1111/j.1365-2184.2007.00503.x.
Oxidative stress is a likely molecular mechanism in long-term diazepam administration. The benefits of antioxidants (melatonin and vitamin C) against diazepam-induced cell proliferation, DNA synthesis and oxidative damage were investigated in this study.
MATERIALS & METHODS: Four equal-sized groups of male rats [control, diazepam (3 mg/kg), diazepam plus melatonin (5 mg/kg) and diazepam plus vitamin C (50 mg/kg)] were used. Levels of lipid peroxides (LPO), superoxide dismutase (SOD) activity and glutathione (GSH) concentration were measured in tissue homogenates. Cell proliferation and rate of DNA synthesis were detected by autoradiography.
Results documented increased labelling index, (3)H-thymidine incorporation (DNA synthesis), LPO plus decrease in GSH levels and SOD activity in livers of diazepam-administered rats versus those of controls. When melatonin and vitamin C were given to diazepam-administered rats, they almost attenuated the increase of labelling index, DNA synthesis and LPO, and restored the levels of GSH and SOD activity.
These results suggest long-term hazard in use of drugs such as diazepam; they may be toxic and damage terminates in complex liver damage. Furthermore, melatonin and vitamin C may be useful in combating free radical-induced liver injury resulting from hazard and/or repeated diazepam administration.
氧化应激可能是长期使用地西泮的分子机制。本研究探讨了抗氧化剂(褪黑素和维生素C)对抗地西泮诱导的细胞增殖、DNA合成及氧化损伤的作用。
将雄性大鼠分为四组,每组数量相等[对照组、地西泮组(3mg/kg)、地西泮加褪黑素组(5mg/kg)和地西泮加维生素C组(50mg/kg)]。测定组织匀浆中脂质过氧化物(LPO)水平、超氧化物歧化酶(SOD)活性和谷胱甘肽(GSH)浓度。通过放射自显影检测细胞增殖和DNA合成速率。
结果表明,与对照组相比,给予地西泮的大鼠肝脏中标记指数、³H-胸腺嘧啶掺入量(DNA合成)增加,LPO增加,GSH水平和SOD活性降低。当给给予地西泮的大鼠同时给予褪黑素和维生素C时,它们几乎减弱了标记指数、DNA合成和LPO的增加,并恢复了GSH水平和SOD活性。
这些结果表明长期使用地西泮这类药物存在危害;它们可能具有毒性,损伤最终导致复杂的肝损伤。此外,褪黑素和维生素C可能有助于对抗因使用地西泮产生的危害和/或反复使用地西泮引起的自由基诱导的肝损伤。